Clinical Data Manager

The post involves collation and/or collection of clinical data, transcription of clinical trial data into trial specific databases, communication with the study team and study sponsors, developing tools to support protocol specific data-capturing, maintaining study specific files, archive the studies, work with team for study audits, and support study team in meeting data locks. The role requires familiarity with medical terminology and a comprehensive approach to processing trial data and also ability to work under pressure.

Key Requirements

Applications are invited from candidates with a health/science related higher education qualification or relevant experience in clinical trials, who possess excellent organisational skills, strong interpersonal and communication skills and high level of time management skills. The successful candidate will be computer literate and will preferably have previous experience in oncology or clinical trial research or extensive experience in healthcare administration.

Appointments will be on a one-year contract in the first instance. To apply for this post, please submit an online application including a supporting statement, detailing reasons why you are applying for the post and with your CV.